Different sectors answer to different rules. We work across the product categories and import pathways where compliance decides whether you reach the market at all.
Class I to III devices and in-vitro diagnostics, across CE Marking, ISO 13485 and FDA 510(k).
Industrial machinery, electrical equipment and electronic products entering the European market.
Personal protective equipment, toys and consumer goods subject to EU product safety requirements.
US importers of human and animal food meeting FDA Foreign Supplier Verification requirements.
CE Marking applies across a wide range of product categories, not only those above. If your product is destined for the European market, we can identify which Directives and Regulations apply and what conformity requires.